BRight DCB First-in-Human Study

Clinical Trial Summary

The primary aim of this clinical study is to assess the safety and clinical performance of the BRight drug-coated balloon (DCB) in the treatment of lower limb arteries stenosis in subjects with Peripheral Artery Disease (PAD). The primary endpoint will be Late Lumen Loss (LLL) of the target lesion at 6 months.

See also
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NCT number	NCT04525794
Study type	Interventional
Source	Biotronik CRC Inc.
Contact
Status	Completed
Phase	N/A
Start date	February 4, 2021
Completion date	February 2, 2024

BRight DCB First-in-Human Study

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms